chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4224752546224752547TC21GENIChomozygous592314987
4224752565224752578CCGTTCCTTTCAT-------------26GENIChomozygous725668066
4224753229224753230GA25GENIChomozygous592314988
4224753689224753690CCA23GENIChomozygous725668067
4224754005224754006GA36GENIChomozygous592314989
4224755022224755023CG29GENIChomozygous594880764
4224755128224755129GGA12GENICpossibly homozygous725668068
4224758154224758156CG--6GENICheterozygous725668070
4224758589224758590TTG20GENIChomozygous725668071
4224758655224758656AG24GENIChomozygous592314990
4224758950224758951TC30GENIChomozygous594880765